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Incomplete Kawasaki disease in patients younger than 1 year of age: a possible inherent risk factor

Authors
Yeo, YunkuKim, TaeYeonHa, KeeSooJang, GiYoungLee, JungHwaLee, KwangChulSon, ChangSungLee, JooWon
Issue Date
2월-2009
Publisher
SPRINGER
Keywords
Kawasaki disease; Infants; Coronary abnormalities; Incomplete manifestation
Citation
EUROPEAN JOURNAL OF PEDIATRICS, v.168, no.2, pp.157 - 162
Indexed
SCIE
SCOPUS
Journal Title
EUROPEAN JOURNAL OF PEDIATRICS
Volume
168
Number
2
Start Page
157
End Page
162
URI
https://scholar.korea.ac.kr/handle/2021.sw.korea/120658
DOI
10.1007/s00431-008-0722-1
ISSN
0340-6199
Abstract
Kawasaki disease (KD) patients younger than 1 year of age are at especially high risk of developing coronary artery abnormalities (CAA). To define the clinical characteristics of this group, as well as the risk factors predisposing them to CAA, we reviewed the medical records of 136 KD patients younger than 1 year of age who were treated at the Korea University Medical Center from January 2001 to July 2006. Of these patients, 16 developed CAA (11.8%). The CAA(+) group had a longer duration of total fever than the CAA(-) group (9.1 +/- 3.7 days vs. 6.3 +/- 2.0 days, p=0.011), but did not differ in the duration of pre- and post-intravenous gamma-globulin (IVGG) fever. The CAA(+) group had fewer diagnostic symptoms than the CAA(-) group (2.7 +/- 1.1 vs. 4.3 +/- 1.2, p < 0.001). Of the hematological findings, the CAA(+) group only differed from the CAA(-) group in having significantly higher total white blood cell (19.2 +/- 6.0 vs. 14.7 +/- 4.7 K/mm(3), p=0.007) and platelet (462.9 +/- 101.0 vs. 383.6 +/- 121.1 K/mm(3), p=0.014) levels. Multivariable logistic regression analysis showed that the only factors which were significantly associated with the development of CAA were the total number of symptoms (OR=0.493, 95% CI=0.293-0.829, p=0.007) and the duration of total fever (OR=1.405, 95% CI=1.092-1.808, p=0.008). Conclusively, incomplete clinical manifestations and a longer duration of total fever are significantly associated with the development of CAA in KD patients younger than 1 year of age. Therefore, these patients should be monitored for incomplete KD, especially if unexplained fever continues, and treatment to shorten the duration of total fever should be initiated.
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